Buttress attachment features for surgical stapling apparatus

ABSTRACT

An end effector assembly for use with a surgical stapler, comprising a staple cartridge having a tissue contacting surface, an anvil plate having a tissue contacting surface, a buttress material releasably disposed on the tissue contacting surfaces of each of the staple cartridge and the anvil plate, and an epoxy positioned onto the tissue contacting surfaces of each of the staple cartridge and anvil plate defining an attachment zone configured to retain the respective buttress material atop the respective tissue contacting surfaces.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of and priority to U.S. ProvisionalPatent Application Ser. No. 61/684,846, filed Aug. 20, 2012, the entiredisclosure of which is incorporated by reference herein.

BACKGROUND

1. Technical Field

The present disclosure relates to surgical stapling apparatuses andbuttress materials for use with said surgical stapling apparatus and,more particularly, to structures and methods for attaching a buttressmaterial to a surgical stapling apparatus.

2. Background of Related Art

Surgical stapling apparatus are employed by surgeons to sequentially orsimultaneously apply one or more rows of fasteners, e.g., staples ortwo-part fasteners, to body tissue for the purpose of joining segmentsof body tissue together. Such apparatus generally include a pair of jawsor finger-like structures between which the body tissue to be joined isplaced. When the stapling apparatus is actuated, or “fired”,longitudinally moving firing bars contact staple drive members in one ofthe jaws. The staple drive members push the surgical staples through thebody tissue and into an anvil in the opposite jaw which forms thestaples. If tissue is to be removed or separated, a knife blade can beprovided in the jaws of the apparatus to cut the tissue between thelines of staples.

For most procedures, the use of bare staples, with the staples in directcontact with the patient's tissue, is generally acceptable. In certainprocedures, the use of surgical supports, e.g., meshes or buttressmaterials, are employed by surgeons in combination with linear orannular stapling devices to bridge, repair and/or reinforce tissuedefects within a patient, especially those occurring in the abdominalwall, chest wall, diaphragm, and other musculo-aponeurotic areas of thebody. The buttress material tends to reinforce the staple or suture lineas well as cover the juncture of the tissues to reduce leakage prior tohealing. In certain minimally invasive surgical procedures the buttressmaterial may be pre-attached to the surgical instrument being used. Forexample, the buttress material can be attached to a staple cartridge oranvil plate of a surgical stapling instrument by the manufacturer.

A surgical stapling apparatus having a surgical buttress releasablysecured thereto by at least one anchor is disclosed in InternationalPublished Application No. WO 08/109,125 A1, the disclosure of which ishereby incorporated by reference herein in its entirety. The buttress isattached to the apparatus by at least one anchor and includes knifeblades for severing the anchors.

U.S. Pat. No. 5,441,193 to Gravener, the disclosure of which is herebyincorporated by reference herein in its entirety, discloses a surgicaldevice having a sheet of curved resilient material attached thereto.Elongated projections can be fixed within slots using adhesive bondingand perforations permit tearing of the film to separate the centralportion of the film from the side portions.

It would be desirable to provide improved means of securely attaching asurgical buttress to the staple cartridge or anvil plate while allowingthe buttress material to fully release from the surgical staplingapparatus after the staples have been fired.

SUMMARY

Disclosed herein is a surgical stapling apparatus including a buttressmaterial and a method of attaching the buttress material to the surgicalstapling apparatus.

In one embodiment of present application a system for securing surgicalbuttresses to the jaws of the stapler is disclosed. The system allowsthe surgical buttresses to be secured to the staple cartridge and/oranvil plate by utilizing ultraviolet light curable epoxy to adhere thesurgical buttresses to a tissue contacting surface of the staplecartridge and/or anvil plate. Perforations may be provided around thelocation of the epoxy to allow the surgical buttress to release from thetissue contacting surfaces by the force applied by the grasp of staplesin the surgical buttress.

In accordance with one embodiment of the present disclosure, the use ofultraviolet light curable epoxy allows the same attachment means to beutilized for both the metal based anvil plate and metal or non-metalstaple cartridge. In addition, the use of ultraviolet light curableepoxy can be precisely controlled both in terms of spatial placement andvolume of deposition as to not impact the anvil plate or staplecartridge. Most importantly, the ultraviolet light curable epoxy isessentially part of the stapling device as it does not detach with thesurgical material and is not implanted into the body.

In another embodiment of the present disclosure, surgical buttresses aresecured to the staple cartridge and/or anvil plate with the use ofretaining members placed through at least one hole of the surgicalbuttress and through at least one opening of at least one of the staplecartridge and/or anvil plate.

In one aspect of the present disclosure, a staple cartridge for use witha surgical stapling apparatus is disclosed. The staple cartridgeincludes a cartridge body including a tissue contacting surface defininga plurality of staple retaining slots. The tissue contacting surface ofthe cartridge body is fabricated from a first material. The staplecartridge further includes a staple disposed within each stapleretaining slot of the cartridge body. A buttress material is releasablydisposed on the tissue contacting surface of the cartridge body and anepoxy is positioned on the tissue contacting surface of the cartridgebody defining an attachment zone configured to retain the buttressmaterial atop the tissue contacting surface.

In an aspect of the present disclosure, the epoxy is an ultravioletlight curable epoxy.

In an aspect of the present disclosure, the tissue contacting surfacehas a first and second outer edge.

In an aspect of the present disclosure, the tissue contacting surfacehas a distal end such that a distal attachment zone is positioned fromthe first outer edge to the second outer edge.

In an aspect of the present disclosure, the tissue contacting surfacehas a proximal end such that a first proximal attachment zone ispositioned parallel to the first outer edge and second proximalattachment zone is positioned parallel to the second outer edge.

In an aspect of the present disclosure, the staple cartridge defines acentral longitudinal slot configured to enable passage of a knife bladetherethrough.

In an aspect of the present disclosure, the first and second proximalattachment zones are positioned distally from a proximal end of thecentral longitudinal slot.

In an aspect of the present disclosure, the distal attachment zone ispositioned proximally for a distal end of the central longitudinal slot.

In an aspect of the present disclosure, the buttress material hasperforations at the proximal end of the tissue contacting surface suchthat the perforations are positioned perpendicularly and distally fromthe first and second proximal attachment zone.

In an aspect of the present disclosure, the buttress material hasperforations at the distal end of the tissue contacting surface suchthat the perforations are positioned parallel and proximal from the atleast one distal attachment zone.

In an aspect of the present disclosure, a plurality of attachment zonesare disposed intermittently along the first and second outer edges.

In an aspect of the present disclosure, the plurality of attachmentzones are concentric.

In an aspect of the present disclosure, the buttress material hasperforations such that the perforations surround the plurality ofattachment zones.

In an aspect of the present disclosure, an end effector assembly for asurgical stapler is disclosed. The end effector including a staplecartridge having a tissue contacting surface, the tissue contactingsurface of the cartridge body being fabricated from a first material.The end effector further including an anvil plate having a tissuecontacting surface, the tissue contacting surface of the anvil platebeing fabricated from a second material that is dissimilar from thefirst material. A buttress material is releasably disposed on the tissuecontacting surfaces of each of the staple cartridge and the anvil plateand an epoxy positioned onto the tissue contacting surfaces of each ofthe staple cartridge and anvil plate defining an attachment zoneconfigured to retain the respective buttress material atop therespective tissue contacting surfaces.

In an aspect of the present disclosure, a surgical stapling apparatus isdisclosed. The apparatus includes a cartridge body including a tissuecontacting surface defining a plurality of staple retaining slots and astaple disposed with each staple retaining slot of the cartridge body.The staple cartridge further includes a substantially circular buttressmaterial releasably disposed on the tissue contacting surface of thecartridge body, the buttress material including an inner peripheraledge, an outer peripheral edge, and a middle portion extending betweenthe inner and outer peripheral edges and an epoxy positioned on thetissue contacting surface of the cartridge body defining an attachmentzone configured to retain the buttress material atop the tissuecontacting surface. In certain preferred embodiments, the epoxy is acurable epoxy, and may be curable upon exposure to ultraviolet light.

The buttress material may further include perforations arranged to allowthe buttress material to separate from the cartridge body. A retainingmember may also be disposed in a hole in the surgical staplingapparatus.

In a further aspect of the present disclosure, a method of assembling asurgical stapling apparatus comprises: providing a surgical staplingapparatus having at least one tissue contacting surface, the tissuecontacting surface having a stapling zone and at least one attachmentzone; applying epoxy on the at least one attachment zone on the tissuecontacting surface; applying a buttress to the tissue contacting surfaceso as to contact at least a portion of the buttress with the epoxy, thebuttress having a portion for overlying the stapling zone and a portionoverlying the attachment zone for being permanently attached to thetissue contacting surface; and curing the epoxy.

The epoxy may be curable with exposure to ultraviolet light. In certainembodiments, the surgical stapling apparatus has an anvil plate and astaple cartridge. The surgical stapling apparatus can be selected fromthe group consisting of a circular surgical stapler and a linearsurgical stapler. The method can include disposing a retaining member ina hole in the surgical stapling apparatus.

Any of the above aspects of the present disclosure described may becombined with any other aspect of the present disclosure withoutdeparting from the scope of the present disclosure.

In another aspect of the present disclosure, a tool assembly for use ina surgical stapling apparatus for joining tissue portions is disclosed.The tool assembly includes a staple cartridge containing a plurality ofsurgical staples therein and an anvil plate configured to cooperate withthe staple cartridge to grasp tissue disposed therebetween where atleast one of the staple cartridge and the anvil plate includes at leastone opening. The tool assembly further includes a buttress materialsupported on the at least one of the staple cartridge and the anvilplate and including at least one hole formed therein. The tool assemblyfurther includes at least one retaining member extending through the atleast one hole and the at least one opening. The retaining member isconfigured to releasably secure the buttress material to the at leastone of the staple cartridge and the anvil plate and is configured toseparate from the buttress material to release the buttress materialfrom the at least one of the staple cartridge and the anvil plate afterfiring of the surgical stapling apparatus.

In an aspect of the present disclosure, the at least one retainingmember includes a pair of buttons and a tether extending therebetween.The tether extends through the at least one hole and the at least oneopening with one of the buttons disposed adjacent each of the at leastone hole and the at least one opening to releasably secure the buttressmaterial to the at least one of the staple cartridge and the anvilplate.

In an aspect of the present disclosure, the pair of buttons are sizedsuch that a diameter of each button is larger than the respective holeor opening.

In an aspect of the present disclosure, the at least one of the staplecartridge and the anvil plate includes a tissue contacting surface and aside surface. The buttress material includes a flap extending beyond thetissue contacting surface and configured for placement adjacent the sidesurface. The flap includes the at least one hole extending therethroughand the at least one opening is disposed in the side surface such thatthe at least one retaining member releasably secures the flap to theside surface.

In an aspect of the present disclosure, the surgical stapling apparatusis a linear surgical stapling apparatus.

In an aspect of the present disclosure, the at least one hole includes aplurality of holes longitudinally spaced along the buttress material.

In an aspect of the present disclosure, the at least one hole includes aplurality of holes spaced along the buttress material transverse to alongitudinal axis of the tool assembly.

In an aspect of the present disclosure, the at least one hole isdisposed adjacent to a corner of the buttress material and the at leastone opening extends through a tissue contacting surface of the at leastone of the staple cartridge and the anvil plate.

In an aspect of the present disclosure, the surgical stapling apparatusis a circular surgical stapling apparatus.

In an aspect of the present disclosure, the at least one hole includes aplurality of holes annularly spaced along the buttress material.

In an aspect of the present disclosure, the buttress material includes afirst flap adjacent an inner side surface of the at least one of thestaple cartridge and the anvil plate and a second flap adjacent an outersurface of the at least one of the staple cartridge and the anvil plate.Each of the first and second flaps includes the at least one hole andeach of the inner and outer side surfaces includes the at least oneopening.

In an aspect of the present disclosure, a tissue contacting surface ofthe at least one of the staple cartridge and the anvil plate includes aflange extending radially inward therefrom. The buttress material issupported on the flange and includes the at least one hole adjacent theflange. The flange includes the at least one opening therein.

In an aspect of the present disclosure, the retaining member is formedof a bioabsorbable polymer.

In an aspect of the present disclosure, the retaining member isconfigured to fracture after the plurality of surgical fasteners arefired.

In an aspect of the present disclosure, the retaining member isdissolvable in a body fluid.

In an aspect of the present disclosure, the retaining member dissolvablein saline.

In an aspect of the present disclosure, the retaining member has a melttemperature of about body temperature.

In an aspect of the present disclosure, retaining member has a melttemperature of about 37° C.

In an aspect of the present disclosure, the buttress material includes aplurality of perforations that are configured to allow the retainingmember to separate from the buttress material.

In yet another aspect of the present disclosure, a method of attaching abuttress material to a surgical stapling apparatus during assembly isdisclosed. The method includes the steps of: providing a staplecartridge containing a plurality of surgical staples therein, providingan anvil plate configured to cooperate with the staple cartridge tograsp tissue disposed therebetween, positioning a buttress material onat least one of the staple cartridge and the anvil plate, inserting aretaining member having a first end and a second end through at leastone hole of the buttress material and at least one opening of the atleast one of the staple cartridge and the anvil plate, and melting theretaining member to form a button on each of the first and second endsto releasably secure the buttress material to the at least one of thestaple cartridge and the anvil plate.

In an aspect of the present disclosure, the buttons are formed such thata diameter of each button is larger than the respective hole or opening.

In an aspect of the present disclosure, a surgical stapling apparatusfor joining tissue portions is disclosed. The apparatus includes astaple cartridge having a plurality of surgical staples disposed thereinand at least one opening formed therein. The staple cartridge furtherincludes a buttress material supported on the staple cartridge andincluding at least one hole formed therein and at least one retainingmember extending through the at least one hole and the at least oneopening. The retaining member is configured to releasably secure thebuttress material to the staple cartridge and is configured to separatefrom the buttress material to release the buttress material from thestaple cartridge after firing of the surgical stapling apparatus.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the presently disclosed interlocking buttressretention systems are disclosed herein with reference to the drawings,wherein:

FIG. 1 is a perspective view of a surgical stapling apparatus accordingto an embodiment of the present disclosure;

FIG. 2 is a perspective view, with parts separated, of a staplecartridge of the surgical stapling apparatus of FIG. 1, illustrating asurgical buttress associated therewith;

FIG. 3 is a perspective view, with parts separated, of an anvil plate ofthe surgical stapling apparatus of FIG. 1, illustrating a surgicalbuttress associated therewith;

FIG. 4 is a perspective view of the staple cartridge, illustrating thesurgical buttress affixed to the staple cartridge;

FIG. 5 is a perspective view of the anvil plate, illustrating thesurgical buttress affixed to the anvil plate;

FIG. 6 is a perspective view of a distal end of the surgical staplingapparatus of FIG. 1, shown in use positioned about a tissue section;

FIG. 7 is a cross-sectional view taken along line 7-7 of FIG. 6;

FIG. 8 is a perspective view of the stapled and divided tissue sectionof FIG. 6;

FIG. 9A is a perspective view of an illustrative embodiment of asurgical stapling apparatus in accordance with another embodiment of thepresent disclosure;

FIG. 9B is a side elevational view partially, broken away, of thesurgical stapling apparatus of FIG. 9A;

FIG. 10A is a perspective view of an illustrative embodiment of thestaple cartridge of the surgical stapling apparatus of FIG. 9A includinga surgical buttress in accordance with an embodiment of the presentdisclosure;

FIG. 10B is a top plan view of the staple cartridge and surgicalbuttress illustrated in FIG. 10A;

FIG. 11 is perspective view of an intestinal area of a patient,illustrating a method of positioning the anvil rod and staple cartridgeof the surgical stapling apparatus of FIGS. 9A, 9B, and 10 within theintestinal area;

FIG. 12 is a schematic perspective view of the intestinal area of FIG.11, illustrating the anvil rod mounted to the surgical staplingapparatus;

FIG. 13A is a perspective view of an alternate embodiment of a staplecartridge of the surgical stapling apparatus of FIG. 1, illustrating abuttress material supported thereon;

FIG. 13B is a top, plan view of the buttress material of FIG. 13A,illustrating the buttress material unfolded;

FIG. 14A is a top, cross-sectional view of the cartridge of FIG. 13A,taken along section line 14A-14A of FIG. 13A;

FIG. 14B is a front, cross-sectional view of the staple cartridge ofFIG. 13A, taken along section line 14B-14B of FIG. 13A;

FIG. 15A is a perspective view of another embodiment of a staplecartridge of the annular surgical stapling apparatus of FIG. 1,illustrating a buttress material supported thereon;

FIG. 15B is a top, plan view the buttress material of FIG. 15A;

FIG. 16A is a side, cross-sectional view of the staple cartridge of FIG.15A, taken along section line 16A-16A of FIG. 15A;

FIG. 16B is a front, cross-sectional view of the staple cartridge ofFIG. 15A, taken along section line 16B-16B of FIG. 15A;

FIG. 17A is a perspective view of another embodiment of a staplecartridge of the annular surgical stapling apparatus of FIGS. 9A-9B,illustrating a buttress material supported thereon;

FIG. 17B is a top, plan view the buttress material of FIG. 17A,illustrating the buttress material unfolded;

FIG. 18A is a side, cross-sectional view of the staple cartridge of FIG.17A, taken along section line 18A-18A of FIG. 17A;

FIG. 18B is a top, cross-sectional view of the staple cartridge of FIG.17A, taken along section line 18B-18B of FIG. 17A;

FIG. 19A is a top, plan view of another embodiment of a staple cartridgeof the annular surgical stapling apparatus of FIGS. 9A-9B, illustratinga buttress material supported on a flange of the staple cartridge;

FIG. 19B is a top, plan view the buttress material of FIG. 19A;

FIG. 20A is a side, cross-sectional view of the staple cartridge of FIG.19A, taken along section line 20A-20A of FIG. 19A, illustrating thestaple cartridge having a flange;

FIG. 20B is a side, cross-sectional view of another embodiment of astaple cartridge of FIG. 19A, illustrating the staple cartridge having arelatively wider inner surface;

FIG. 21 is a perspective view of a anvil plate of the surgical staplingapparatus of FIG. 1, illustrating a buttress material supported thereonin accordance with another embodiment of the present disclosure; and

FIG. 22 is a perspective view of a staple cartridge of the annularsurgical stapling apparatus of FIGS. 9A-9B, illustrating a buttressmaterial supported thereon in accordance with another embodiment of thepresent disclosure.

DETAILED DESCRIPTION OF THE EMBODIMENTS

Various exemplary embodiments of the present disclosure are discussedherein below in terms of buttresses for use with surgical staplingapparatus. The buttresses described herein may be used in sealing awound by approximating the edges of wound tissue between a staplecartridge and an anvil plate of a surgical stapling apparatus whichcontains at least one buttress. The at least one buttress is joined tothe surgical stapling apparatus by at least one attachment zone formedby an epoxy positioned between a tissue contacting surface of each ofthe staple cartridge and anvil plate and the least one buttress. Firingof the surgical stapling apparatus forces legs of at least one staple topass through an opening on the staple cartridge, the tissue, and theopenings on the anvil plate to secure the buttress to the tissue, tosecure the adjoining tissue to one another, and to seal the tissue.Thus, the present disclosure describes surgical buttresses, surgicalstapling apparatus supporting said surgical buttresses, and methods andmechanisms for using the same.

It should be understood that a variety of surgical stapling apparatusmay be utilized with a surgical buttress of the present disclosure. Forexample, linear stapler configurations may be utilized, such as, forexample those including Duet TRS™ reloads and staplers with Tri-Staple™technology, available through Covidien, which maintain a principal placeof business at 555 Long Wharf Drive, North Haven, Conn. 06511, andtransverse anastomosis staplers, such as, for example, EEA™, CEEA™,GIA™, EndoGIA™, and TA™ surgical staplers, also available G throughCovidien. It should also be appreciated that the principles of thepresent disclosure are equally applicable to surgical staplers havingalternate configurations, such as, for example, end-to-end anastomosisstaplers having a circular cartridge and anvil (see, e.g., commonlyowned U.S. Pat. No. 5,915,616, entitled “Surgical Fastener ApplyingApparatus,” the entire content of which is incorporated herein by thisreference); laparoscopic staplers (see, e.g., commonly owned U.S. Pat.Nos. 6,330,965 and 6,241,139, each entitled “Surgical StaplingApparatus,” the entire contents of each of which being incorporatedherein by this reference); and transverse anastomosis staplers (see,e.g., commonly owned U.S. Pat. Nos. 5,964,394 and 7,334,717, eachentitled “Surgical Fastener Applying Apparatus”, the entire contents ofeach of which being incorporated herein by this reference).

Embodiments of the presently disclosed surgical buttress and surgicalstapling apparatus will now be described in detail with reference to thedrawing figures wherein like reference numerals identify similar oridentical elements. In the following discussion, the terms “proximal”and “trailing” may be employed interchangeably, and should be understoodas referring to the portion of a structure that is closer to a clinicianduring proper use. The terms “distal” and “leading” may also be employedinterchangeably, and should be understood as referring to the portion ofa structure that is further from the clinician during proper use. Asused herein, the term “patient” should be understood as referring to ahuman subject or other animal, and the term “clinician” should beunderstood as referring to a doctor, nurse, or other care provider andmay include support personnel.

Referring now to FIG. 1, there is disclosed an exemplary surgicalstapling apparatus or surgical stapler 10 for use in stapling tissue andapplying a buttress material or surgical buttress to the tissue. Anexemplary example of this type of surgical stapling instrument isdisclosed in U.S. Pat. No. 7,128,253, the entire disclosure of which isincorporated by reference herein.

Surgical stapling apparatus 10 generally includes a handle 12 having anelongate tubular member 14 extending distally from handle 12. An endeffector assembly 16 is mounted on a distal end 18 of elongate tubularmember 14. End effector assembly 16 includes a staple cartridge 200configured to receive a cartridge body 32 therein and an anvil plate300. End effector assembly 16 may be permanently affixed to elongatetubular member 14 or may be detachable and thus replaceable with a newend effector assembly 16. Anvil plate 300 is movably mounted on distalend 18 of jaw assembly 16 and is movable between an open position spacedapart from staple cartridge 200 to a closed position substantiallyadjacent staple cartridge 200. Anvil plate 300 is fabricated from ametal material, including and not limited to stainless steel, titanium,titanium alloy, and the like. At least a tissue contacting surface ofstaple cartridge 200 is fabricated from a material other than metal,including and not limited to plastic, thermoplastic, resin,polycarbonate, and the like.

Surgical stapling apparatus 10 further includes a trigger 33, as seen inFIG. 1, movably mounted on handle 12. Actuation of trigger 33 initiallyoperates to move anvil plate 300 from the open to the closed positionrelative to staple cartridge 200 and subsequently actuates surgicalstapling apparatus 10 to apply lines of staples to tissue. In order toproperly orient end effector assembly 16 relative to the tissue to bestapled, surgical stapling apparatus 10 is additionally provided with arotation knob 34 mounted on handle 12. Rotation of rotation knob 34relative to handle 12 rotates elongate tubular member 14 and endeffector assembly 16 relative to handle 12 so as to properly orient endeffector assembly 16 relative to the tissue to be stapled.

A driver 36, as seen in FIGS. 6 and 7A, is provided to move anvil plate300 between the open and closed positions relative to staple cartridge200. Driver 36 moves through a longitudinal slot 338 (FIG. 3) formed inanvil plate 300. A knife 30 with knife blade 31 is associated withdriver 36 to cut tissue captured between staple cartridge 200 and anvilplate 300 as driver 36 passes through slot 338. The driver may beconfigured as a beam with an upper portion that engages the anvil plate300 and a lower portion that engages the channel that supports thestaple cartridge 200. For example, U.S. Pat. No. 7,565,993 to Millimanet al., the disclosure of which is hereby incorporated by referenceherein in its entirety, discloses an axial drive assembly 212 includingan elongated drive beam 266 for approximating the anvil and staplecartridge to clamp tissue and fire staples therein. The staplingapparatus 10 can include such a beam, or other known structure. Thestaple cartridge 200 has staple receiving slots for retaining staplestherein, whereas the anvil plate includes staple forming recesses. Thedriver forces the staples from the staple receiving slots and drivesthem into the staple forming recesses so that they are formed into aclosed shape around tissue.

Reference may be made to commonly owned U.S. Pat. Nos. 5,915,616,6,330,965, and 6,241,139, referenced above, for a detailed discussion ofthe construction and operation of an exemplary surgical staplingapparatus 10.

Staple cartridge 200 and/or anvil plate 300 may be provided with asurgical buttress 500. Surgical buttress 500 is provided to reinforceand seal the lines of staples applied to tissue by surgical staplingapparatus 10. Surgical buttress 500 may be configured into any shape,size, or dimension suitable to fit any surgical stapling, fastening, orfiring apparatus.

Staple cartridge 200 is provided with a cartridge buttress 500 a andanvil plate 300 is provided with an anvil buttress 500 b in the mannersdescribed in more detail hereinbelow. The buttresses 500 a, 500 b may bemade from any biocompatible natural or synthetic material. The materialfrom which the buttresses 500 a, 500 b are formed may be bioabsorbableor non-bioabsorbable. It should be understood that any combination ofnatural, synthetic, bioabsorbable and non-bioabsorbable materials may beused to form the buttress material. The buttresses 500 a, 500 b may beporous or non-porous, combination of porous and non-porous layers. Thenon-porous buttresses 500 a, 500 b may be utilized to retard or preventtissue ingrowth from surrounding tissues thereby acting as an adhesionbarrier and preventing the formation of unwanted scar tissue.

Additional exemplary materials for surgical buttresses 500 a, 500 b foruse with the surgical stapling devices disclosed herein are set forth incommonly assigned U.S. Pat. Nos. 5,542,594; 5,908,427; 5,964,774; and6,045,560, and commonly assigned U.S. Application Publication Nos.2006/0085034, filed on Apr. 20, 2006; and 2006/0135992, filed on Jun.22, 2006, the entire contents of each of being hereby incorporatedherein by reference in their entirety.

As illustrated in the current embodiment and shown in FIGS. 2 and 3,surgical buttress 500 is releasably attached to staple cartridge 200and/or anvil plate 300 at attachment zones 240, 340, respectively,defined by strategically positioned ultraviolet (UV) light curable epoxythat affixes surgical buttresses 500 a, 500 b to the inwardly facing ortissue contacting surfaces 220, 320 of the staple cartridge 200 and/orthe anvil plate 300, as discussed in detail below. The use of UV curablyepoxy enables fixing of surgical buttresses 500 a, 500 b to therespective tissue contacting surfaces 220, 320 of staple cartridge 200and anvil plate 300 which are fabricated from dissimilar material.

With reference to FIG. 2, cartridge buttress 500 a of staple cartridge200 is operatively secured or adhered to a tissue contacting surface 220of staple cartridge 200, by epoxy 250 positioned onto both a proximalend 260 and a distal end 262 of the tissue contacting surface 220. Epoxy250 is disposed between the cartridge buttress 500 a and the tissuecontacting surface 220. Staple cartridge 200 further includes a firstouter edge 248 a and second outer edge 248 b. A distal attachment zone240 a (FIG. 4) is disposed distally of a distal end of a centrallongitudinal slot 238 and extends substantially from the first outeredge 248 a to the second outer edge 248 b of staple cartridge 200. Atleast one proximal attachment zone 240 b is disposed proximally of thedistal end of the central longitudinal slot 238. The proximal and distalattachment zones on the staple cartridge are positioned outside the areain which the staple receiving slots are defined in the staple cartridge.

Cartridge buttress 500 a includes perforations 246 that allow cartridgebuttress 500 a to be released from the tissue contacting surface 220.Perforations 246 extend linearly in a direction perpendicular to thecentral longitudinal slot 238 near the proximal and distal attachmentzones 240 a, 240 b. In particular, at the distal end 262 of staplecartridge 200, perforations 246 a of the cartridge buttress 500 a aredisposed between the distal attachment zone 240 a and the distal end ofthe central longitudinal slot 238. Further, at the proximal end 260 ofstaple cartridge 200, the perforations 246 b of the cartridge buttress500 a are disposed distally of each proximal attachment zone 240 b.

With reference to FIG. 3, and similar to cartridge buttress 500 a, anvilbuttress 500 b is operatively secured or adhered to a tissue contactingsurface 320 of anvil plate 300, by epoxy 350 positioned at a proximal360 and distal end 362 of the anvil plate 300 and between the anvilbuttress 500 b and the tissue contacting surface 320 of anvil plate 300.A distal attachment zone 340 a (FIG. 5) is disposed distally of a distalend of a central longitudinal slot 338 and extends substantially betweenthe outer edges 348 a, 348 b of anvil plate 300. At least one proximalattachment zone 342 b is disposed proximally of the distal end of thecentral longitudinal slot 338. The proximal and distal attachment zoneson the anvil plate 300 are positioned outside the area in which thestaple receiving recesses are defined in the anvil plate.

Anvil buttress 500 b includes perforations 346 similar to cartridgebuttress 500 a. Perforations 346 of anvil buttress 500 b extend linearlyin a direction perpendicular to the central longitudinal slot 338 nearthe proximal and distal attachment zones 340 a, 340 b from the first andsecond outer edges 348 a, 348 b. In particular, at the distal end 362 ofanvil plate 300, the perforations 346 a of the anvil buttress 500 b aredisposed between the distal attachment zone 340 a and the distal end ofthe central longitudinal slot 338. Further, at the proximal end 360 ofanvil plate 300, the perforations 346 b of the anvil buttress 500 b aredisposed distally of each proximal attachment zone 340 b. theperforations enable the buttresses 500 a, 500 b to be permanentlyattached to the anvil plate and staple cartridge while allowing therelease of the buttresses after stapling has been performed.

FIGS. 4 and 5 illustrate the buttresses 500 a, 500 b disposed on thestaple cartridge 200 and anvil plate 300, respectively. As shown,additional attachment zones 240 c, 340 c, for respective staplecartridge 200 and anvil plate 300, are disposed along outer edges 248 a,248 b, 348 a, 348 b of each of staple cartridge 200 and anvil plate 300.Perforations 246 c, 346 c surround the attachments zones 240 c, 340 c toallow buttresses 500 a, 500 b to be released from the tissue contactingsurfaces 220, 320. The attachment zones 240 c, 340 c are shown asconcentric but additional shapes and sizes may be contemplated. Theattachment zones in any of the embodiments disclosed herein may haveshapes that are circular, rectangular, oblong, etc., or any appropriateshape. Likewise, the epoxy material in any of the embodiments disclosedherein may have shapes that are circular, rectangular, oblong, etc., orany appropriate shape.

During assembly, epoxy 250, 350 is disposed at predetermined locationson tissue contacting surfaces 220, 320 of each of staple cartridge 200and anvil plate 300 by known methods, such as spraying, dipping,blotting, dabbing, or similar known methods in the art. Once thebuttresses 500 a, 500 b are placed onto each of the tissue contactingsurfaces 220, 320 of staple cartridge 200 and anvil plate 300,respectively, an ultraviolet light is used to cure epoxy 250, 350 andbond buttresses 500 a, 500 b to the epoxy 250, 350 and thus to thetissue contacting surfaces 220, 320. In any of the embodiments disclosedherein, it is contemplated that the epoxy could be partially cured andthen the buttress is adhered to the partially cured epoxy.

In any of the embodiments disclosed herein, the epoxy can be an epoxythat is cured using any electromagnetic radiation, including but notlimited to ultraviolet light.

As illustrated in FIG. 6, during use of surgical stapling apparatus 10,the staple cartridge 200 and anvil plate 300, having surgical buttresses500 a, 500 b loaded thereon (as described above) are positioned oneither side of the surgical site. Tissue contacting surfaces 220, 320 ofstaple cartridge 200 and anvil plate 300 are positioned adjacent layersof tissue “T” to be fastened to one another.

As shown in FIG. 7, staple cartridge 22 includes surgical staples 50positioned within the individual staple retaining slots 52. Staples 50are of a conventional type and include a backspan 54 having a pair oflegs 56 and 58 extending from backspan 54. Legs 56 and 58 terminate intissue penetrating tips 60 and 62, respectively. Pushers 64 are locatedwithin staple retaining slots 52 and are positioned between staples 50and the path of a drive bar 66.

Surgical stapling apparatus 10 is initially actuated by movement oftrigger 33 relative to handle 12 (FIG. 1) causing driver 36 to move inthe direction of arrow “A” (FIG. 6), and against sloped edge 21 of anvilplate 300 thereby causing anvil plate 300 to be moved to the closedposition relative to staple cartridge 200. As drive bar 66 advancesdistally within staple cartridge 32, drive bar 66 urges pushers 64upwardly against backspan 54 of staples 50 driving legs 56 and 58 ofstaples 50 through the cartridge buttresses 500 a, tissue “T”, and anvilbuttress 500 b, towards staple forming pockets 68 in anvil plate 300.Tissue penetrating tips 60 and 62 of staple legs 56 and 58 are bentwithin staple forming pockets 68 in anvil plate 20 with backspan 54securing surgical buttress 24 against tissue “T”. The buttresses 500 a,500 b tear along the perforations 246, 346 thereby breaking the bondsformed by the epoxy 250, 350 and releasing the buttresses 500 a, 500 bfrom the tissue contacting surfaces 220, 320 of each of the staplecartridge 200 and anvil plate 300. In this manner, epoxy 250, 350remains on the tissue contacting surfaces 220, 320 as the buttresses 500a, 500 b detach. The epoxy is not implanted into the body but is removedwith the stapling apparatus.

Upon full actuation of surgical stapling apparatus 10, a knife 30associated with surgical stapling apparatus 10 and carried by driver 36may be utilized to cut tissue “T”, as well as surgical buttresses 500 a,500 b between the rows of now formed staples 50. Upon movement of anvilplate 300 to the open position spaced apart from staple cartridge 200,surgical buttresses 500 a, 500 b finish pulling away from tissuecontacting surfaces 220, 320 from staple cartridge 200 and anvil plate300 along the perforations 246, 346.

The resulting tissue “T”, divided and stapled closed with staples 50, isillustrated in FIG. 8. Specifically, surgical buttresses 500 a, 500 bare secured against tissue “T” by legs 56, 58 and backspans 54 ofstaples 50. Thus, surgical buttresses 500 a, 500 b are stapled to tissue“T” thereby sealing and reinforcing the staple lines created by staples50.

Referring now to FIGS. 9A and 9B, an annular surgical stapling apparatus110, for use with surgical buttresses 124 of the present disclosure, isshown. Surgical stapling apparatus 110 includes a handle assembly 112having at least one pivotable actuating handle member 133, and anadvancing member 135. Extending from handle member 112, there isprovided a tubular body portion 114 which may be constructed so as tohave a curved shape along its length. Body portion 114 terminates in astaple cartridge 122 which includes a pair of annular arrays of stapleretaining slots 152 having a staple 150 disposed in each one of stapleretaining slots 152. Positioned distally of staple cartridge 122 thereis provided an anvil assembly 120 including an anvil member 121 and ashaft 123 operatively associated therewith for removably connectinganvil assembly 120 to a distal end portion of stapling apparatus 110.

Staple cartridge 122 may be fixedly connected to the distal end oftubular body portion 114 or may be configured to concentrically fitwithin the distal end of tubular body portion 114. Staple cartridge 122includes a staple pusher 164 including a proximal portion having agenerally frusto-conical shape and a distal portion defining twoconcentric rings of peripherally spaced fingers (not shown), each one ofwhich is received within a respective staple retaining slot 152.

A knife 130, substantially in the form of an open cup with the rimthereof defining a knife blade 131, is disposed within staple cartridge122 and mounted to a distal surface of a staple pusher 164. The knife130 is disposed radially inward of the pair of annular arrays of staples150. Accordingly, in use, as the staple pusher 164 is advanced, theknife 130 is also advanced axially outward.

As seen in FIG. 10A, a surgical buttress 124 is releasably attached tothe staple cartridge 122 at attachment zones 140 defined by deposits ofepoxy 150 disposed between the surgical buttress 124 and the tissuecontacting surface 134 of the staple cartridge 122. As described hereinabove, epoxy 150 bonds the surgical buttress 124 to the tissuecontacting surface 134. Perforations 146 surround each deposit of epoxy150 to allow surgical buttress 124 to release from tissue contactingsurface 134. Surgical buttress 124 is provided in an annularconfiguration and includes a central aperture 125 to receive shaft 123of anvil assembly 120 therethrough. As illustrated, the attachment zones140 are concentric in an annular configuration about an outer peripheraledge 162 and inner peripheral edge 160 of staple cartridge 122.

It is envisioned that the surgical buttress 124 may be additionally oralternatively attached or adhered to tissue contacting surface of anvilplate 121 in a manner similar to the surgical buttress 124 attached tostaple cartridge 122.

As shown in FIG. 10B, surgical buttress 124 may be secured or adhered tothe staple cartridge 122 along an inner portion or peripheral edge 160and outer portion or peripheral edge 162 of surgical buttress 124. It isenvisioned that other configurations may be utilized to retain thesurgical buttress 124 to the staple cartridge 122, such as providing theattachment zones 140 along either the inner or outer annular row ofstaple retaining slots 152, or alternating the attachment zones 140between the staple retaining slots 152, or among other arrangementswithin the purview of those skilled in the art.

Surgical stapling apparatus 110 and detachable anvil assembly 120 areused in an anastomosis procedure to effect joining of intestinalsections 50 and 52. The anastomosis procedure is typically performedusing minimally invasive surgical techniques including laparoscopicmeans and instrumentation. At the point in the procedure shown in FIG.11, a diseased intestinal section has been previously removed, anvilassembly 120 (optionally including a surgical buttress 124 thereon) hasbeen applied to the operative site either through a surgical incision ortransanally and positioned within intestinal section 52, and tubularbody portion 114 of surgical stapling apparatus 110 (optionallyincluding a surgical buttress 124 thereon) has been inserted transanallyinto intestinal section 50. Intestinal sections 50 and 52 are also showntemporarily secured about their respective components (e.g., shaft 123of anvil assembly 120, and the distal end of tubular body portion 114)by conventional means such as a purse string suture “P”, as illustratedin FIG. 12.

Thereafter, the clinician maneuvers anvil assembly 120 until theproximal end of shaft 123 is inserted into the distal end of tubularbody portion 114 of surgical stapling apparatus 110, wherein themounting structure (not shown) within the distal end of tubular bodyportion 114 engages shaft 123 to effect the mounting. Anvil assembly 120and tubular body portion 114 are then approximated to approximateintestinal sections 50, 52. Surgical stapling apparatus 110 is thenfired. A knife (not shown) cuts the portion of tissue and surgicalbuttress 124 disposed radially inward of the knife, to complete theanastomosis. The anvil assembly 120 and staple cartridge 122 are opened,with surgical buttress 124 stapled to intestinal sections 50 and 52.Surgical buttress 124 tears away from the deposits of epoxy 150, alongperforations 146.

With reference now to FIGS. 13A, 13B, 14A and 14B an alternateembodiment is shown wherein buttress material 1000 is disposed on thetissue contacting surface 2200 of staple cartridge 2000 by a pair offlaps 1020, or margins of material that are positioned adjacent sidesurfaces 2320 of staple cartridge 2000. Staple cartridge 2000 is similarto staple cartridge 200 discussed hereinabove having tissue contactingsurface 2200 and a plurality of retention slots 2380 formed therein forretaining a plurality of staples or fasteners 2400 therein. Any of theembodiments disclosed herein can include the flaps or margins forattaching buttress material.

Buttress material 1000 is disposed on the tissue contacting surface 2200of staple cartridge 2000 over the openings 2380 a of retention slots2380. Buttress material 1000 includes a pair of flaps 1020 positionedadjacent side surfaces 2320 of staple cartridge 2000 and includes atleast one hole 1040 extending through each of flaps 1020. Each hole 1040is longitudinally spaced apart from the next along the length of arespective flap 1020. Staple cartridge 2000 further includes at leastone opening 2480 in each of side surfaces 2320 where each opening 2480corresponds to a respective one of the holes 1040 of buttress material1000. In one embodiment, when buttress material 1000 is disposed ontissue contacting surface 2200, holes 1040 of buttress material 1000substantially align or are in registration with the correspondingopenings 2480 of staple cartridge 2000.

With reference now to FIGS. 14A and 14B, a retaining member 1060 extendsthrough each hole 1040 of buttress material 1000 and correspondingopening 2480 of staple cartridge 2000 to secure buttress material 1000to staple cartridge 2000. Retaining member 1060 includes a pair ofbuttons 1080 linked together by a shaft or tether 1100. Tether 1100extends through one of openings 2480 and the corresponding hole 1040such that a first button 1080 a is disposed adjacent an inner surface2320 a of staple cartridge 2000 and a second button 1080 b is disposedadjacent an outer surface 1120 of buttress material 1000. Each button1080 is sized to be larger than a respective opening 2480 or hole 1040to inhibit removal of the retaining member 1060 from the opening 2480and hole 1040 during use. The retaining member may have other shapes,including hooks, loops, or tabs. In certain embodiments, the retainingmember has bulbous ends that facilitate snapping the retaining memberthrough the holes 2480 and 1040.

Retaining members 1060 may be formed of a bio-compatible or bioabsorbable material. In one embodiment, retaining members 1060 may beconfigured to be brittle and absorbable such that, upon firing ofsurgical stapling apparatus 10, retaining members 1060 are fractured torelease buttress material 1000 from staple cartridge 2000. In anotherembodiment, retaining members 1060 may be dissolvable upon applicationof a subsequent fluid by the surgeon or by a surgical instrument, e.g. asaline fluid, during use in order to release buttress material 1000 fromstaple cartridge 2000. Retaining members 1060 may also or alternativelybe dissolvable by body fluids in order to release buttress material1000. In another embodiment, retaining members 1060 may be formed of anabsorbable polymer or other similar low melt temperature material thatis configured to melt or soften at body temperature, e.g., about 37° C.,to release buttress material 1000 from staple cartridge 2000. In any ofthe embodiments disclosed herein, retaining members that are integrallyformed with the buttress material may be used to attach the buttress tothe anvil or staple cartridge of a stapling apparatus.

With reference now to FIGS. 15A, 15B, 16A and 16B, in another embodimentbuttress material 2100 is disposed on the tissue contacting surface 2200of staple cartridge 2000 over the openings 2380 a of retention slots2380. Buttress material 2100 includes a proximal end 2600 and a distalend 2620. Each of proximal and distal ends 2600, 2620 includes at leastone hole 2060 and preferably two holes 2060 extending therethrough. Forexample, in one embodiment, buttress material 2100 may be substantiallyrectangular with each hole 2060 disposed proximate to a corner 2080 ofbuttress material 2100. Staple cartridge 2000 further includes at leastone opening 2050 through tissue contacting surface 2200 where eachopening 2050 corresponds to a respective one of the holes 2060 ofbuttress material 2100. In one embodiment, when buttress material 2100is disposed on tissue contacting surface 2200, holes 2060 of buttressmaterial 2100 substantially align or are in registration with thecorresponding openings 2050 of staple cartridge 2000.

With reference now to FIGS. 16A and 16B, one of retaining members 1060extends through each hole 2060 of buttress material 2100 andcorresponding opening 2050 of staple cartridge 2000 to secure buttressmaterial 2100 to staple cartridge 2000, as described above. For example,tether 1100 of retaining member 1060 extends through one of openings2050 and the corresponding hole 2060 such that the first button 1080 ais disposed adjacent an inner surface 2200 a of tissue contactingsurface 2200 and the second button 1080 b is disposed adjacent an outersurface 2010 of buttress material 2100. Each button 1080 is sized to belarger than a respective opening 2050 or hole 2060 to inhibit removal ofthe retaining member 1060 from the opening 2050 or hole 2060 during use.

It is contemplated that a buttress material 1000 or 2100 may also oralternatively be disposed on anvil assembly in the same manner asdescribed above with regard to the attachment of buttress materials 1000and 2100 to staple cartridge 2000.

With reference now to FIGS. 17A-20B buttress material is shown asgenerally annular in shape for securing to an annular surgical staplingapparatus 110 as discussed in FIGS. 9A and 9B. Referring now to FIGS.17A, 17B, 18A and 18B, a buttress material 4000 is generally annular inshape and includes an inner portion 4020, a middle portion 4040, and anouter portion 4060. A substantially centrally located aperture 4080,defined by the inner circumference of inner portion 4020 is formedthrough buttress material 4000. Buttress material 4000 may be any shapesufficient to provide support for anastomosis of tissue after surgicalstapling apparatus 110 has been fired including, for example, a square,a circle, an oval, a triangle or any other polygonal or other shape.

Buttress material 4000 is sized such that when buttress material 4000 ispositioned over tissue contacting surface 3360 of staple cartridge 3200,buttress material 4000 extends radially beyond inner surface 3200 a andouter surface 3200 b of staple cartridge 3200 such that inner portion4020 and outer portion 4060 of buttress material 4000 may be folded overto abut or engage inner and outer surfaces 3200 a, 3200 b, respectively.

Each of inner portion 4020 and outer portion 4060 includes an annulararray of holes 4412, 4416, respectively, and inner and outer surfaces3200 a and 3200 b include corresponding openings 3240, 3260,respectively for the reception of retaining members 1060 therethrough.For example, when buttress 4000 is positioned on tissue contactingsurface 3360 with inner and outer portions 4020, 4060 folded over toabut inner and outer surfaces 3200 a, 3200 b, respectively, the holes4120, 4160 and the corresponding openings 3240, 3260 may besubstantially radially aligned or in registration.

With reference now to FIGS. 18A and 18B, one of retaining members 1060extends through each hole 4120, 4160 of each of inner and outer portions4020, 4060, respectively and through the corresponding openings 3240,3260 of staple cartridge 3200 to secure buttress material 4000 to staplecartridge 3200. For example, the tether 1100 of a respective retainingmember 1060 extends through one of openings 3240 of inner surface 3200 aand through the corresponding hole 4120 of inner portion 4020 ofbuttress material 4000 such that the first button 1080 a is disposedadjacent an inside portion 3250 of inner surface 3200 a and the secondbutton 1080 b is disposed adjacent an outer surface 4020 a of innerportion 4020 of buttress material 4000. Likewise, the tether 1100 ofanother retaining member 1060 extends through one of openings 3260 ofouter surface 3200 b and through the corresponding hole 4120 of outerportion 4060 such that the first button 1080 a is disposed adjacent aninside portion 3270 of outer surface 3200 b and the second button 1080 bis disposed adjacent an outer surface 4060 a of outer portion 4060. Eachbutton 1080 is sized to be larger than a respective opening 3240, 3260or hole 4120, 4160 to inhibit removal of the retaining member 1060 fromthe opening 3240, 3260 or hole 4120, 4160 during use.

With reference now to FIGS. 19A, 19B, 20A and 20B, in one embodiment, abuttress material 5000, formed of similar materials to buttress material4000, described above, is generally annular in shape and includes aninner portion 5020, a middle portion 5040, and an outer portion 5060. Asubstantially centrally located aperture 5080, defined by the innercircumference of inner portion 5020 is formed through buttress material5000. Buttress material 5000 may be any shape sufficient to providesupport for anastomosis of tissue after surgical stapling apparatus 110has been fired including, for example, a square, a circle, an oval, atriangle or any other polygonal or other shape.

With reference now to FIGS. 19A, 19B, and 20A, in one embodiment,buttress material 5000 is sized such that when buttress material 5000 ispositioned over tissue contacting surface 3360 of staple cartridge 3200,the outer edge 5060 a of outer portion 5060 of buttress material 5000 issubstantially aligned with outer surface 3200 b of staple cartridge 3200and inner edge 5020 a of inner portion 5020 extends radially inward ofthe inner surface 3200 a of staple cartridge 3200. Staple cartridge 3200includes a flange 3480 extending radially inward from tissue contactingsurface 3360. Inner portion 5020 of buttress material 5000 includes anannular array of holes 5100, and flange 3480 includes a correspondingannular array of openings 3500 for the reception of retaining members1060 therethrough. For example, when buttress 5000 is positioned ontissue contacting surface 3360 with inner portion 5020 extendingradially inward of inner surface 3200 a, inner portion 5020 ispositioned on flange 3480 and the holes 5100 and the correspondingopenings 3500 in flange 3480 may be substantially aligned or inregistration, e.g., longitudinally aligned.

One of retaining members 1060 extends through each hole 5100 of innerportion 5020 and through the corresponding openings 3500 of flange 3480to secure buttress material 5000 to staple cartridge 3200. For example,the tether 1100 of a respective retaining member 1060 extends throughone of openings 3500 of flange 3480 and through the corresponding hole5100 of inner portion 5020 of buttress material 5000 such that the firstbutton 1080 a is disposed adjacent a proximal surface 3480 a of flange3480 and the second button 1080 b is disposed adjacent a distal surface5020 a of inner portion 5020 of buttress material 5000. Each button 1080is sized to be larger than a respective opening 3500 or hole 5100 toinhibit removal of the retaining member 106 from the opening 3500 orhole 5100 during use.

With reference now to FIG. 20B, in another embodiment, staple cartridge3200 may include an inner surface 3520 having a greater radial thicknessthan inner surface 3200 a of staple cartridge 3200 illustrated in FIG.20A such that a distal portion 3520 a of inner surface 3520 of staplecartridge 3200 extends radially inward from tissue contacting surface3360. Similar to flange 3480 above, distal portion 3520 a of innersurface 3520 of staple cartridge 3200 includes an annular array ofopenings 3540 corresponding to the holes 5100 of buttress material 5000.For example, when buttress 5000 is positioned on tissue contactingsurface 3360, inner portion 5020 is positioned on the distal portion3520 a of inner surface 3520 such that the holes 5100 and thecorresponding openings 3540 may be substantially aligned, e.g.,longitudinally aligned or in registration.

One of retaining members 1060 extends through each hole 5100 of innerportion 5020 of buttress material 5000 and through the correspondingopenings 3540 of the distal portion 3520 a of the inner surface 3520 ofstaple cartridge 3200 to secure buttress material 5000 to staplecartridge 3200. For example, the tether 1100 of a respective retainingmember 1060 extends through one of openings 3540 of the distal portion3520 a of inner surface 3520 of staple cartridge 3200 and through thecorresponding hole 5100 of inner portion 5020 of buttress material 5000such that the first button 1080 a is disposed proximal of the opening3540 in distal portion 3520 a and the second button 1080 b is disposedadjacent a distal surface 5020 a of inner portion 5020 of buttressmaterial 5000. Each button 1080 is sized to be larger than a respectiveopening 3540 or hole 5100 to inhibit removal of the retaining member1060 from the opening 3540 or hole 5080 during use.

Referring now to FIGS. 13A, 15A, 17A and 19A, in any of the aboveembodiments, buttress materials 1000, 2100, 4000 and 5000 may includeperforations or breakaway sections 1140, 2140, 4140, 5140 that areconfigured to release the buttress material 1000, 2100, 4000, 5000 fromthe cartridge assemblies 2000, 3200. For example, buttress material 1000may include perforations extending longitudinally along the fold line offlaps 1020, buttress material 2100 may include perforations extendingtransverse to the longitudinal axis adjacent the holes 2060 of theproximal and distal portions 2600, 26200, buttress material 4000 mayinclude perforations extending radially along the fold lines of one orboth of inner portion 4020 and outer portion 4060, and buttress material5000 may include an annular array of perforations disposed radiallyoutward of holes 5100 relative to a longitudinal axis of the staplecartridge 3200. Alternatively, or in addition, each of holes 1040, 2060,4120, 4160 and 5100 may include perforations or break away sections suchthat buttons 1080 a, 1080 b of a retaining member 1060 may break throughor snap through holes 1040, 2060, 4120, 4160 and 5100 as buttressmaterial 1000, 2100, 4000, 5000 is released from cartridge assemblies2000, 3200.

Referring now to FIGS. 21 and 22, in one embodiment, it is contemplatedthat a buttress material 1000, 2100, 4000 and 5000 may alternatively oradditionally be removably secured to one of anvil assemblies 2202, and3220 in a similar manner as described in the above embodiments forremovable securement of buttress materials 1000, 2100, 4000 and 5000 tocartridge assemblies 2000 and 3200.

In one embodiment, retaining members 1060 may be formed during assemblyof the surgical stapling apparatus or placement of buttress material tothe surgical stapling apparatus 10, 110 during the manufacture orassembly thereof. In a method of attaching the buttress material to asurgical stapling apparatus, the polymer is deposited onto the buttressmaterial, the polymer material having a melting temperature lower thanthe melting temperature of the buttress material. The polymer can bedeposited by injection molding, spraying, dipping, or other methods. Inthis way, the polymer material can be melted without disrupting thephysical properties of the buttress material. In an embodiment of thepresent disclosure, the degradable polymer material for the attachmentfeatures is the polymer used in making Caprosyn™ sutures, also known asL25, which has a melt temperature of about 125 to about 145 degreescelcius, while the buttress material is L41 or L21, which have meltingtemperatures of about 210 to about 220 degrees celcius and about 185 toabout 200 degrees celcius respectively. The L21 polymer is used to makeMaxon™ sutures. The polymer L41 is similar to L21, but has a differentchemical structure, and has a greater degree of crystallinity and ahigher glass transition temperature and melting temperature. Both L21and L41 are a copolymer of glycolide and trimethylene carbonate.

In certain embodiments, the top of the driver 36 mechanically disruptsthe interlocking features of the bonding polymer and may shear off aportion of the polymer material. In certain embodiments, the knifesevers off a portion of the polymer material that attaches the buttressmaterial to the apparatus. In certain embodiments, small pushers areprovided in the staple cartridge, which are actuated along with thestaple firing pushers, to release the buttress material from theapparatus. In further embodiments, additional cutting assemblies can beprovided in the anvil, staple cartridge, or both.

In any of the embodiments disclosed herein, the buttress material or thepolymer of the attachment zone or attachment feature can be made fromglycolic acid, glycolide, lactic acid, lactide, dioxanone,epsilon-caprolactone, trimethylene carbonate, etc., as is known in theart.

Persons skilled in the art will understand that the devices and methodsspecifically described herein and illustrated in the accompanyingfigures are non-limiting exemplary embodiments, and that thedescription, disclosure, and figures should be construed merelyexemplary of particular embodiments. It is to be understood, therefore,that the present disclosure is not limited to the precise embodimentsdescribed, and that various other changes and modifications may beeffected by one skilled in the art without departing from the scope orspirit of the disclosure. Additionally, it is envisioned that theelements and features illustrated or described in connection with oneexemplary embodiment may be combined with the elements and features ofanother exemplary embodiment without departing from the scope of thepresent disclosure, and that such modifications and variations are alsointended to be included within the scope of the present disclosure.Accordingly, the subject matter of the present disclosure is not to belimited by what has been particularly shown and described, except asindicated by the appended claims.

What is claimed is:
 1. A staple cartridge for use with a surgicalstapling apparatus, the staple cartridge comprising: a cartridge bodyincluding a tissue contacting surface defining a plurality of stapleretaining slots, the tissue contacting surface of the cartridge bodybeing fabricated from a first material; a staple disposed within eachstaple retaining slot of the cartridge body; a buttress materialreleasably disposed on the tissue contacting surface of the cartridgebody; and an epoxy positioned on the tissue contacting surface of thecartridge body defining an attachment zone configured to retain thebuttress material atop the tissue contacting surface.
 2. The staplecartridge of claim 1, wherein the epoxy is an ultraviolet light curableepoxy.
 3. The staple cartridge of claim 2, wherein the tissue contactingsurface has a first and second outer edge.
 4. The staple cartridge ofclaim 3, wherein the tissue contacting surface has a distal end suchthat a distal attachment zone is positioned from the first outer edge tothe second outer edge.
 5. The staple cartridge of claim 4, wherein thetissue contacting surface has a proximal end such that a first proximalattachment zone is positioned parallel to the first outer edge andsecond proximal attachment zone is positioned parallel to the secondouter edge.
 6. The staple cartridge of claim 5, wherein the staplecartridge defines a central longitudinal slot configured to enablepassage of a knife blade therethrough.
 7. The end effector of claim 6,wherein the first and second proximal attachment zones are positioneddistally from a proximal end of the central longitudinal slot.
 8. Theend effector of claim 6, wherein the distal attachment zone ispositioned proximally for a distal end of the central longitudinal slot.9. The staple cartridge of claim 7, wherein the buttress material hasperforations at the proximal end of the tissue contacting surface suchthat the perforations are positioned perpendicularly and distally fromthe first and second proximal attachment zone.
 10. The staple cartridgeof claim 8, wherein the buttress material has perforations at the distalend of the tissue contacting surface such that the perforations arepositioned parallel and proximal from the at least one distal attachmentzone.
 11. The staple cartridge of claim 3, wherein a plurality ofattachment zones are disposed intermittently along the first and secondouter edges.
 12. The staple cartridge of claim 11, wherein the pluralityof attachment zones are concentric.
 13. The staple cartridge of claim12, wherein the buttress material has perforations such that theperforations surround the plurality of attachment zones.
 14. An endeffector assembly for a surgical stapler, the end effector comprising:the staple cartridge according to claim 1, the tissue contacting surfaceof the cartridge body being fabricated from a first material; an anvilplate having a tissue contacting surface, the tissue contacting surfaceof the anvil plate being fabricated from a second material that isdissimilar from the first material; a buttress material releasablydisposed on the tissue contacting surfaces of each of the staplecartridge and the anvil plate; and an epoxy positioned onto the tissuecontacting surfaces of each of the staple cartridge and anvil platedefining an attachment zone configured to retain the respective buttressmaterial atop the respective tissue contacting surfaces.
 15. The endeffector of claim 14, wherein the staple cartridge and the anvil platehave a central longitudinal slot configured to enable passage of a knifeblade therethrough.
 16. The end effector of claim 14, wherein thebuttress material on each of the tissue contacting surfaces of each ofthe staple cartridge and the anvil plate has perforations positionedperpendicular to the central longitudinal slot.
 17. A surgical staplingapparatus, comprising: a cartridge body including a tissue contactingsurface defining a plurality of staple retaining slots; a stapledisposed with each staple retaining slot of the cartridge body; asubstantially circular buttress material releasably disposed on thetissue contacting surface of the cartridge body, the buttress materialincluding an inner peripheral edge, an outer peripheral edge, and amiddle portion extending between the inner and outer peripheral edges;and an epoxy positioned on the tissue contacting surface of thecartridge body defining an attachment zone configured to retain thebuttress material atop the tissue contacting surface.
 18. The surgicalstapling apparatus of claim 18, wherein the epoxy is an ultravioletlight curable epoxy.
 19. The surgical stapling apparatus of claim 18,wherein the buttress material includes perforations arranged to allowthe buttress material to separate from the cartridge body.